Canonical Allele Identifier: CA2686682444

Gene: EPHX2

Linked Data

• gnomAD v4: 8-27501160-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27501160A>G , CM000670.2:g.27501160A>G	GRCh38
NC_000008.10:g.27358677A>G , CM000670.1:g.27358677A>G	GRCh37
NC_000008.9:g.27414594A>G	NCBI36
NG_012064.1:g.15033A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521400.6:c.186+150A>G MANE Select	ENSP00000430269.1:n.186+150A>G
ENST00000380476.7:c.27+150A>G	ENSP00000369843.3:n.27+150A>G
ENST00000517536.5:c.186+150A>G	ENSP00000428875.1:n.186+150A>G
ENST00000518328.5:c.186+150A>G	ENSP00000430779.1:n.186+150A>G
ENST00000518379.5:c.186+150A>G	ENSP00000427956.1:n.186+150A>G
ENST00000520623.5:n.270+150A>G
ENST00000520666.1:n.198+150A>G
ENST00000521400.5:c.186+150A>G	ENSP00000430269.1:n.186+150A>G
ENST00000521684.1:c.185+150A>G
ENST00000521780.5:c.-12-2444A>G	ENSP00000430302.1:n.-12-2444A>G
ENST00000523827.1:n.409+150A>G
NM_001256482.1:c.27+150A>G	NP_001243411.1:n.27+150A>G
NM_001256483.1:c.-12-2444A>G	NP_001243412.1:n.-12-2444A>G
NM_001256484.1:c.27+150A>G	NP_001243413.1:n.27+150A>G
NM_001979.5:c.186+150A>G	NP_001970.2:n.186+150A>G
XM_017013199.1:c.186+150A>G	XP_016868688.1:n.186+150A>G
XM_017013200.1:c.186+150A>G	XP_016868689.1:n.186+150A>G
XR_001745491.1:n.244+150A>G
NM_001256482.2:c.27+150A>G	NP_001243411.1:n.27+150A>G
NM_001256483.2:c.-12-2444A>G	NP_001243412.1:n.-12-2444A>G
NM_001256484.2:c.27+150A>G	NP_001243413.1:n.27+150A>G
NM_001979.6:c.186+150A>G MANE Select	NP_001970.2:n.186+150A>G